chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116829702	116829703	T	C	45	GENIC	homozygous	116670288
8	116830227	116830228	A	T	31	GENIC	homozygous	118090540
8	116836553	116836554	G	A	55	GENIC	homozygous	117149257
8	116838551	116838552	A	G	30	GENIC	homozygous	116670296
8	116839090	116839091	T	C	54	GENIC	homozygous	116670298
8	116839135	116839136	C	G	51	GENIC	homozygous	116670300
8	116839379	116839380	C	T	50	GENIC	homozygous	117149259
8	116844118	116844119	G	A	53	GENIC	homozygous	116886737
8	116844434	116844435	T	C	57	GENIC	homozygous	116670310
8	116844768	116844769	A	G	60	GENIC	homozygous	116670312
8	116844898	116844899	C	G	59	GENIC	homozygous	117149261
8	116846254	116846255	C	T	32	GENIC	homozygous	116670320
8	116846255	116846256	C	G	31	GENIC	homozygous	116670322
8	116846569	116846570	C	T	45	GENIC	homozygous	117149262
8	116847770	116847771	A	G	58	GENIC	homozygous	116670324
8	116850249	116850250	T	A	56	GENIC	homozygous	116670330
8	116852060	116852061	C	A	33	GENIC	homozygous	116670336
8	116854037	116854038	T	C	22	GENIC	homozygous	116670342
8	116854207	116854208	G	A	28	GENIC	homozygous	116670344
8	116854831	116854832	C	T	42	GENIC	homozygous	116886743